bio-biomart-queries — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-biomart-queries (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
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Reference examples tested with: pybiomart 0.9+, R biomaRt 2.58+ (Bioconductor); Ensembl BioMart (release 110+)
Before using code patterns, verify installed versions match. If versions differ:
pip show pybiomartpackageVersion('biomaRt')The BioMart XML query format is stable across Ensembl releases; the underlying mart names and attribute IDs can change between Ensembl releases. For published work, pin the Ensembl release via useEnsembl(version=110).
"Bulk-convert IDs / pull coordinate tables / extract ortholog wide tables" -> BioMart is the right answer for any Ensembl-rooted query producing >5,000 rows. It is a separate service from the Ensembl REST API, with separate rate behavior and a different query model (XML-based, batch-oriented). For one-off lookups (<100 records), Ensembl REST is more convenient; for bulk anything, BioMart wins.
The single most important fact: BioMart returns a flat table from a single query. There is no per-record loop, no rate-limit cascade, no async polling. One XML query in; one TSV out.
pybiomart (https://github.com/jrderuiter/pybiomart) is the lightest clientbiomaRt Bioconductor (Durinck et al. 2009 Nat Protoc 4:1184) is the canonical clientcurl against the XML endpoint works but is rarely used directlyhttps://www.ensembl.org/biomart/martview for interactive query designpip install pybiomart pandas
# R:
# BiocManager::install('biomaRt')| Level | Examples |
|---|---|
| Mart | ENSEMBL_MART_ENSEMBL (genes), ENSEMBL_MART_SNP (variants), ENSEMBL_MART_MOUSE (mouse-specific) |
| Dataset | hsapiens_gene_ensembl, mmusculus_gene_ensembl, etc. (per species) |
| Attribute | Fields to return: ensembl_gene_id, external_gene_name, chromosome_name, etc. |
| Filter | Constraints on the query: chromosome_name = 17, biotype = protein_coding, etc. |
A query is: pick a mart, pick a dataset, list attributes to return, list filters to constrain. BioMart returns a single TSV.
Discovery:
from pybiomart import Server
server = Server(host='http://www.ensembl.org')
print(server.marts) # list marts
mart = server['ENSEMBL_MART_ENSEMBL']
print(mart.datasets) # list datasets (species)
ds = mart['hsapiens_gene_ensembl']
print(ds.attributes) # list attributes
print(ds.filters) # list filters| Question | BioMart | Ensembl REST |
|---|---|---|
| Bulk ID mapping (>5000 IDs) | yes (1 query) | rate-limited cascade |
| Single-gene lookup | overkill | yes |
| Coordinate tables for thousands of genes | yes | rate-limited |
| Ortholog wide-table across species | yes (multi-species mart) | per-gene loop |
| VEP variant annotation | no | yes (or local VEP) |
| Sequence retrieval | partial | yes |
| Real-time | no (batch) | yes (per-record) |
| Reproducibility (version pin) | useEnsembl(version=110) | archive URL e110.rest.ensembl.org |
For >5K rows, BioMart is the right tool. For real-time per-record lookups, REST.
| Attribute | Returns |
|---|---|
ensembl_gene_id | Stable Ensembl Gene ID |
ensembl_gene_id_version | With .N version suffix |
external_gene_name | HGNC symbol (or species-equivalent) |
hgnc_id, hgnc_symbol | HGNC permanent ID and symbol |
entrezgene_id | NCBI Gene ID |
refseq_mrna, refseq_peptide | RefSeq accessions |
uniprotswissprot, uniprotsptrembl | UniProt accessions |
chromosome_name, start_position, end_position, strand | Gene coordinates |
transcript_count, exon_count | Counts |
biotype | protein_coding, lncRNA, miRNA, etc. |
description | Free-text gene description |
go_id, name_1006, namespace_1003 | GO term ID, name, namespace |
| Filter | Constraint |
|---|---|
ensembl_gene_id | List of Gene IDs |
external_gene_name | List of symbols |
entrezgene_id | List of NCBI Gene IDs |
chromosome_name | One or more chromosomes |
start / end | Coordinate range |
biotype | One or more biotypes |
with_<source> | Boolean: has cross-ref to <source> (e.g. with_hpa = has Human Protein Atlas) |
Goal: Convert 5,000 Ensembl Gene IDs to HGNC symbols, RefSeq mRNA accessions, and UniProt accessions in one query.
Approach: pybiomart query with three attributes; ID list as a filter; returns one TSV.
Reference (pybiomart 0.9+, Ensembl release 110+):
from pybiomart import Server
import pandas as pd
server = Server(host='http://www.ensembl.org')
mart = server['ENSEMBL_MART_ENSEMBL']
ds = mart['hsapiens_gene_ensembl']
ensembl_ids = ['ENSG00000139618', 'ENSG00000141510', 'ENSG00000171862'] # ...up to 5K+
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name', 'hgnc_id',
'refseq_mrna', 'uniprotswissprot'],
filters={'ensembl_gene_id': ensembl_ids},
)
print(df.head())
# One row per (gene, cross-ref) pair; genes with multiple RefSeq mRNAs get multiple rows.df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name', 'chromosome_name',
'start_position', 'end_position', 'strand', 'biotype'],
filters={'chromosome_name': '17', 'biotype': 'protein_coding'},
)
print(f'{len(df)} protein-coding genes on chr17')Goal: One TSV with human Ensembl ID, mouse ortholog Ensembl ID, zebrafish ortholog Ensembl ID per row.
Approach: Ortholog attributes from the human mart query both species' orthologs.
df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name',
'mmusculus_homolog_ensembl_gene', 'mmusculus_homolog_orthology_type',
'drerio_homolog_ensembl_gene', 'drerio_homolog_orthology_type'],
filters={'chromosome_name': '17'},
)
# pybiomart columns use the mart display names, which can vary across releases.
# Resolve column names defensively rather than hardcoding strings:
mouse_type_col = next(c for c in df.columns if 'Mouse' in c and 'type' in c)
zebra_type_col = next(c for c in df.columns if 'Zebrafish' in c and 'type' in c)
df_one2one = df[(df[mouse_type_col] == 'ortholog_one2one') &
(df[zebra_type_col] == 'ortholog_one2one')]
print(f'{len(df_one2one)} 1:1 orthologs across all three species on chr17')df = ds.query(
attributes=['ensembl_gene_id', 'external_gene_name',
'go_id', 'name_1006', 'namespace_1003'],
filters={'external_gene_name': ['TP53', 'BRCA1', 'MYC', 'EGFR']},
)
# Long format: one row per (gene, GO term) pair# Reference: Bioconductor biomaRt 2.58+ | Verify API if version differs
library(biomaRt)
# Pin to release 110 for reproducibility
ensembl <- useEnsembl(biomart='genes', dataset='hsapiens_gene_ensembl', version=110)
# Or via host URL (for older or specific assemblies)
# ensembl <- useMart('ENSEMBL_MART_ENSEMBL',
# dataset='hsapiens_gene_ensembl',
# host='https://nov2020.archive.ensembl.org')
df <- getBM(
attributes = c('ensembl_gene_id', 'external_gene_name', 'entrezgene_id',
'uniprotswissprot', 'refseq_mrna'),
filters = 'ensembl_gene_id',
values = c('ENSG00000139618', 'ENSG00000141510'),
mart = ensembl
)
head(df)# What attributes are available?
attrs = ds.attributes
ortho_attrs = [a for a in attrs if 'homolog' in a]
print(f'{len(ortho_attrs)} ortholog attributes; first 5: {ortho_attrs[:5]}')
# What filters?
filts = ds.filters
chrom_filts = [f for f in filts if 'chrom' in f]useMart('ensembl', ...) without version=.useEnsembl(version=110) or archive host URL.ensembl_gene_id, refseq_mrna; a gene with 10 RefSeq mRNAs produces 10 rows.ensembl_canonical filter where available.filters={'external_gene_name': ['MARCH1']} post-2020.ensembl_gene_id or hgnc_id; these are stable.mmusculus_homolog_ensembl_gene for 30K human genes./lookup/symbol calls.ENSEMBL_MART_SNP.server.marts; pick ENSEMBL_MART_ENSEMBL for genes.| Error / symptom | Cause | Solution |
|---|---|---|
| Empty result | Wrong attribute / filter name | List with ds.attributes and ds.filters |
| Timeout on big query | No filter, too many rows | Chunk by chromosome |
| Drift between re-runs | No version pinning | useEnsembl(version=110) |
| Row count > expected | Many-to-many cross-ref joins | Filter to canonical isoform |
| Symbol filter returns nothing | HGNC rename | Filter by Ensembl ID or HGNC ID |
| Slow on ortholog wide-table | Multi-species join expensive | Chunk by chromosome |
~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.